Variant #0000525313 (NC_000005.9:g.176831231C>G, NM_000505.3:c.984G>C (F12))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.176831231C>G
DNA change (hg38) g.177404230C>G
Published as F12(NM_000505.3):c.984G>C (p.T328=)
ISCN -
DB-ID F12_000017
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-29 09:18:44 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F12 NM_000505.3 -?/. 9 c.984G>C r.(?) p.(Thr328=)
PFN3 NM_001029886.2 -?/. - c.-3654G>C r.(?) p.(=)


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